Anaplasma marginale major surface protein 3 is encoded by a polymorphic, multigene family
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Updated: Nov 3, 2026

Oncogenic Gene Fusion Detection Using Anchored Multiplex Polymerase Chain Reaction Followed by Next Generation Sequencing
Published on: July 5, 2019
A R Alleman1, G H Palmer, T C McGuire
1Department of Physiological Sciences, University of Florida, Gainesville 32610, USA. ARALL@GNV.IFAS.UFL.EDU
Abstract:
The immunodominant surface protein, MSP3, is structurally and antigenically polymorphic among strains of Anaplasma marginale. In this study we show that a polymorphic multigene family is at least partially responsible for the variation seen in MSP3. The A. marginale msp3 gene msp3-12 was cloned and expressed in Escherichia coli. With msp3-12 as a probe, multiple, partially homologous gene copies were identified in the genomes of three A. marginale strains. These copies were widely distributed throughout the chromosome. Sequence analysis of three unique msp3 genes, msp3-12, msp3-11, and msp3-19, revealed both conserved and variant regions within the open reading frames. Importantly, msp3 contains amino acid blocks related to another polymorphic multigene family product, MSP2. These data, in conjunction with data presented in previous studies, suggest that multigene families are used to vary important antigenic surface proteins of A. marginale. These findings may provide a basis for studying antigenic variation of the organism in persistently infected carrier cattle.
Insights
Anaplasma marginale uses a polymorphic multigene family to vary its surface protein MSP3, contributing to antigenic variation. This genetic diversity may explain persistent infections in cattle.
Area of Science:
- Veterinary Microbiology
- Molecular Biology
- Immunology
Background:
- Anaplasma marginale, a significant cattle pathogen, exhibits antigenic variation in its surface proteins.
- The immunodominant surface protein, MSP3, shows considerable structural and antigenic polymorphism across different strains.
Purpose of the Study:
- To investigate the genetic basis of MSP3 polymorphism in Anaplasma marginale.
- To determine if multigene families contribute to the antigenic variation of MSP3.
Main Methods:
- Cloning and expression of the A. marginale msp3-12 gene in Escherichia coli.
- Using msp3-12 as a probe to identify homologous gene copies in A. marginale genomes.
- Sequence analysis of identified msp3 gene variants.
Main Results:
- Multiple, partially homologous msp3 gene copies were detected in the genomes of three A. marginale strains.
- These msp3 gene copies were distributed throughout the bacterial chromosome.
- Sequence analysis revealed conserved and variant regions within msp3 genes, with some amino acid blocks related to MSP2.
Conclusions:
- A polymorphic multigene family is at least partially responsible for the variation in Anaplasma marginale's MSP3 protein.
- Multigene families are likely employed by A. marginale to vary key antigenic surface proteins.
- These findings offer insights into the antigenic variation mechanisms driving persistent infections in carrier cattle.
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